This phase II trial is studying 18F-fluoromisonidazole and fludeoxyglucose F 18 PET/CT scans to see how well they work in assessing oxygen in tumor tissue of patients with soft tissue sarcoma undergoing chemotherapy with or without radiation therapy. Using diagnostic procedures, such as 18F-fluoromisonidazole and fludeoxyglucose F 18 PET scan and CT scan, to find oxygen in tumor cells may help in planning cancer treatment. It may also help doctors predict how well a patient will respond to treatment.
PRIMARY OBJECTIVES: I. Evaluate the potential of 18F-fluoromisonidazole (\[18F\] FMISO) as a non-invasive indicator of tissue hypoxia to provide tumor-imaging data that correlates with tissue markers of hypoxia in patients with soft tissue sarcoma treated with neoadjuvant chemotherapy with or without radiotherapy. SECONDARY OBJECTIVES: I. Test \[18F\] FMISO tumor uptake as an independent predictor of patient outcome and if it provides additional predictive power over fludeoxyglucose F 18 PET scan. II. Test \[18F\] FMISO tumor uptake as a predictor of response in the subgroup of patients treated with radiotherapy and chemotherapy. III. Test the reproducibility of \[18F\] FMISO uptake in tumors by imaging the same patients on sequential days in a test-retest protocol. IV. Determine the relationship between hypoxia-related biomarkers (HIF1-a and VEGF), proliferation biomarkers (microvascular density, p53, and Ki-67), and regional \[18F\] FMISO uptake in tumor. OUTLINE: Patients undergo fludeoxyglucose F 18 \[18F\] FDG and 18F-fluoromisonidazole (\[18F\] FMISO) positron emission tomography (PET)/CT scans before starting neoadjuvant chemotherapy (without or without radiotherapy) and after completion of 4 courses of neoadjuvant therapy. NOTE: Some patients may undergo repeat \[18F\] FMISO PET/CT scan within 48 hours after the first \[18F\] FMISO scan to evaluate the variability (test-retest) of this imaging measurement. Blood samples are collected after completion of \[18F\] FMISO and \[18F\] FDG PET/CT scans for laboratory biomarker studies by IHC assays. Tumor samples from biopsy or surgery are also collected for biomarker studies. After completion of study procedures, patients are followed up periodically for 2 years.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
8
Undergo 18F FDG and 18F FMISO PET/CT scans
Undergo 18F FDG and 18F FMISO PET/CT scans
Undergo 18F FDG and 18F FMISO PET/CT scans
Undergo 18F FDG and 18F FMISO PET/CT scans
Correlative studies
Seattle Cancer Care Alliance
Seattle, Washington, United States
University of Washington Medical Center
Seattle, Washington, United States
Changes From Baseline Hypoxic Volume (HV)
ANOVA and Kruskal-Wallis analysis will be performed across the different categories to look for significant associations.
Time frame: Baseline and up to 2 years
Overall Survival
Multivariate Cox regression will be used. The outcome is binary and generalized linear models and logistic regression will be employed.
Time frame: Up to 2 years
Disease Free Survival
Multivariate Cox regression will be used.
Time frame: From start of treatment to the follow-up review where recurrent disease is first detected, assessed up to 2 years
Response to Radiation Therapy (XRT) by RECIST Criteria
Will be approached using multivariate logistic regression.
Time frame: Up to 2 years
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